alström syndrome…

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alström syndrome, inherited disease characterized by progressive blindness, deafness, early-onset type 2 diabetes mellitus, obesity, intelligence is not affected, alström syndrome, autosomal recessive inherited disorder, that a person must inherit a copy, the defective gene from both parents, extremely rare, more common in holland, sweden than, mutated gene, alms1, was, not yet known how this gene causes, blindness, severe vision impairment in infancy, symptoms of childhood-onset, type 2 diabetes, obesity, deafness, dark patches of skin, acanthosis nigricans, growth retardation, impaired heart function, cardiomyopathy, lead to heart failure, progressive kidney failure, hypothyroidism, liver dysfunction, small penis, gastrointestinal reflux, , eyes, examined, ophthalmologist, standard ophthalmic examination, reduced visual ability, blood tests, chem-20, an elevation of serum triglycerides, hyperglycemia, high blood sugar, tests evaluating thyroid function abnormal, high tsh, low free t4, hearing tests abnormal, tests of heart function, echocardiogram, abnormal, , no specific treatment, syndrome, diabetes, oral medications, insulin, of both, cholesterol, medications, hearing, augmented, hearing aids, heart abnormalities, medications ace inhibitors, beta-blockers, spironolactone, given to improve heart function, hypothyroidism, thyroid hormone replacement, alström syndrome international, 14 whitney farm road, mount desert, maine 04660, permanent blindness, deafness is likely to develop, type 2 diabetes develops, kidney, liver failure, progress, complications related to diabetes, impaired heart function, untreated, lead to fatigue, shortness of breath, diabetes, high cholesterol increase the risk of coronary artery disease, call health care provider, suspect symptoms of diabetes increased thirst, urination, seek medical attention promptly, suspect that infant, child cannot see, hear, .